@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP686122.RAitA_eolk7CjS4zxoM7J8bquW_LkpjGJUs0Yk-_kr4aA130_head { this: np:hasAssertion dgn-np:NP686122.RAitA_eolk7CjS4zxoM7J8bquW_LkpjGJUs0Yk-_kr4aA130_assertion; np:hasProvenance dgn-np:NP686122.RAitA_eolk7CjS4zxoM7J8bquW_LkpjGJUs0Yk-_kr4aA130_provenance; np:hasPublicationInfo dgn-np:NP686122.RAitA_eolk7CjS4zxoM7J8bquW_LkpjGJUs0Yk-_kr4aA130_publicationInfo; a np:Nanopublication . dgn-np:NP686122.RAitA_eolk7CjS4zxoM7J8bquW_LkpjGJUs0Yk-_kr4aA130_assertion a np:Assertion . dgn-np:NP686122.RAitA_eolk7CjS4zxoM7J8bquW_LkpjGJUs0Yk-_kr4aA130_provenance a np:Provenance . dgn-np:NP686122.RAitA_eolk7CjS4zxoM7J8bquW_LkpjGJUs0Yk-_kr4aA130_publicationInfo a np:PublicationInfo . } dgn-np:NP686122.RAitA_eolk7CjS4zxoM7J8bquW_LkpjGJUs0Yk-_kr4aA130_assertion { miriam-gene:6530 a ncit:C16612 . lld:C0264423 a ncit:C7057 . dgn-gda:DGN3b2d0d6eb4b824b4e8712be79f198553 sio:SIO_000628 miriam-gene:6530, lld:C0264423; a sio:SIO_001121 . } dgn-np:NP686122.RAitA_eolk7CjS4zxoM7J8bquW_LkpjGJUs0Yk-_kr4aA130_provenance { dgn-np:NP686122.RAitA_eolk7CjS4zxoM7J8bquW_LkpjGJUs0Yk-_kr4aA130_assertion dcterms:description "[Association studies on NAT1 and NAT2 polymorphisms focused in this review indicate the genetic significance of slow acetylation phenotype in bronchial and occupational asthma as well as in other allergic diseases in different populations worldwide.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:18680475; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP686122.RAitA_eolk7CjS4zxoM7J8bquW_LkpjGJUs0Yk-_kr4aA130_publicationInfo { this: dcterms:created "2016-05-13T12:46:56+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }